Does DULOXETINE Cause Adulterated product? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Adulterated product have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.0% of all adverse event reports for DULOXETINE.
17
Reports of Adulterated product with DULOXETINE
0.0%
of all DULOXETINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Adulterated product From DULOXETINE?
Of the 17 reports.
Is Adulterated product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does DULOXETINE Cause?
Nausea (7,355)
Dizziness (6,983)
Drug withdrawal syndrome (6,503)
Headache (5,541)
Fatigue (5,309)
Insomnia (5,270)
Anxiety (4,973)
Paraesthesia (4,854)
Drug ineffective (4,829)
Hyperhidrosis (4,101)
What Other Drugs Cause Adulterated product?
LISDEXAMFETAMINE DIMESYLATE (31)
THEOBROMINE (29)
ACETAMINOPHEN (28)
LIDOCAINE (28)
COCAINE (27)
CAFFEINE (24)
CODEINE (23)
THEOPHYLLINE (23)
FENTANYL (22)
MORPHINE (22)
Which DULOXETINE Alternatives Have Lower Adulterated product Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB